Concept explainers
(a)
Interpretation:
The hybridization and approximate bond angle for each carbon atoms in
Concept Introduction:
Hybridization is the mixing of valence atomic orbitals to get equivalent hybridized orbitals that having similar characteristics and energy.
Geometry of different types of molecule with respect to the hybridizations are mentioned are mentioned below,
Bond angle is the angle between two bonds of a molecule and it is determined based on the electron-domain geometry.
(a)
Explanation of Solution
Given molecule is
The Lewis electron dot structure for alanine is given below:
.
Consider the first carbon. There will be four electron regions in the molecule and hence the electron-region geometry will be tetrahedral. For a molecule having tetrahedral geometry, the hybridization will be
Consider the second carbon. There will be four electron regions in the molecule and hence the electron-region geometry will be tetrahedral. For a molecule having tetrahedral geometry, the hybridization will be
Consider the third carbon. There will be two electron regions in the molecule and hence the electron-region geometry will be linear. For a molecule having linear geometry, the hybridization will be
Consider the fourth carbon atom. There will be two electron regions in the molecule and hence the electron-region geometry will be linear. For a molecule having linear geometry, the hybridization will be
(b)
Interpretation:
The shortest carbon-to-carbon bond length in molecule has to be identified.
Concept Introduction:
Bond length is the distance between the nuclei in a bond and it is related to the sum of the covalent radii at the bonded atoms.
Higher the bond order, shorter will be the bond length.
(b)
Explanation of Solution
Given molecule is
The Lewis electron dot structure for alanine is given below:
.
In the given molecule, the triple bond is present between
(c)
Interpretation:
The strongest carbon-to-carbon bond length in molecule has to be identified.
Concept Introduction:
Comparing triple bond, double bond and single bond, the bond with higher energy is the triple bond.
(c)
Explanation of Solution
Given molecule is
The Lewis electron dot structure for alanine is given below:
.
In the given molecule, the triple bond is present between
The strength of a triple bond is more than the single bond.
Thus, the strongest carbon-to-carbon bond is between
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Chapter 7 Solutions
OWLv2 for Moore/Stanitski's Chemistry: The Molecular Science, 5th Edition, [Instant Access], 1 term (6 months)
- For each of the following, indicate whether the arrow pushes are valid. Do we break any rules via the arrows? If not, indicate what is incorrect. Hint: Draw the product of the arrow and see if you still have a valid structure. a. b. N OH C. H N + H d. e. f. مه N COHarrow_forwardDecide which is the most acidic proton (H) in the following compounds. Which one can be removed most easily? a) Ha Нь b) Ha Нь c) CI CI Cl Ha Ньarrow_forwardProvide all of the possible resonanse structures for the following compounds. Indicate which is the major contributor when applicable. Show your arrow pushing. a) H+ O: b) c) : N :O : : 0 d) e) Оarrow_forward
- Draw e arrows between the following resonance structures: a) b) : 0: :0: c) :0: N t : 0: بار Narrow_forwardDraw the major substitution products you would expect for the reaction shown below. If substitution would not occur at a significant rate under these conditions, check the box underneath the drawing area instead. Be sure you use wedge and dash bonds where necessary, for example to distinguish between major products. Note for advanced students: you can assume that the reaction mixture is heated mildly, somewhat above room temperature, but strong heat or reflux is not used. Cl Substitution will not occur at a significant rate. Explanation Check :☐ O-CH + Х Click and drag to start drawing a structure.arrow_forwardDraw the major substitution products you would expect for the reaction shown below. If substitution would not occur at a significant rate under these conditions, check the box underneath the drawing area instead. Be sure you use wedge and dash bonds where necessary, for example to distinguish between major products. Note for advanced students: you can assume that the reaction mixture is heated mildly, somewhat above room temperature, but strong heat or reflux is not used. Cl C O Substitution will not occur at a significant rate. Explanation Check + O-CH3 Х Click and drag to start drawing a structure.arrow_forward
- ✓ aw the major substitution products you would expect for the reaction shown below. If substitution would not occur at a significant rate under these conditions, check the box underneath the drawing area instead. Be sure you use wedge and dash bonds where necessary, for example to distinguish between major products. Note for advanced students: you can assume that the reaction mixture is heated mildly, somewhat above room temperature, but strong heat or reflux is not used. C Cl HO–CH O Substitution will not occur at a significant rate. Explanation Check -3 ☐ : + D Click and drag to start drawing a structure. © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use Privacy Cearrow_forwardPlease correct answer and don't used hand raitingarrow_forwardDon't used hand raiting and don't used Ai solutionarrow_forward
- Determine whether the following reaction is an example of a nucleophilic substitution reaction: Br OH HO 2 -- Molecule A Molecule B + Br 义 ollo 18 Is this a nucleophilic substitution reaction? If this is a nucleophilic substitution reaction, answer the remaining questions in this table. Which of the reactants is referred to as the nucleophile in this reaction? Which of the reactants is referred to as the organic substrate in this reaction? Use a ŏ + symbol to label the electrophilic carbon that is attacked during the substitution. Highlight the leaving group on the appropriate reactant. ◇ Yes O No O Molecule A Molecule B Molecule A Molecule B टेarrow_forwardPlease correct answer and don't used hand raitingarrow_forwardPlease correct answer and don't used hand raitingarrow_forward
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